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Clinical Trial Summary

Registry intended to provide a data repository and reporting infrastructure for the surveillance of CytoSorb device use in real-world critical care settings, and to serve as an objective, comprehensive, and scientifically-based resource to measure and improve the quality of patient care


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Acute Liver Failure
  • Acute Lung Injury
  • Acute on Chronic Liver Failure
  • Acute Respiratory Distress Syndrome
  • Acute-On-Chronic Liver Failure
  • Burns
  • Cardiogenic Shock
  • Communicable Diseases
  • Cytokine Release Syndrome
  • Drug Overdose
  • End Stage Liver Disease
  • Endocarditis
  • Extracorporeal Life Support
  • Hemophagocytic Lymphohistiocytoses
  • Hepatic Insufficiency
  • Infections
  • Infectious Disease
  • Liver Failure
  • Liver Failure, Acute
  • Liver Transplant; Complications
  • Lymphohistiocytosis, Hemophagocytic
  • Pancreatitis
  • Postoperative Vasoplegic Syndrome
  • Respiratory Distress Syndrome
  • Respiratory Distress Syndrome, Newborn
  • Rhabdomyolysis
  • Sepsis
  • Septic Shock
  • Shock
  • Shock, Cardiogenic
  • Syndrome
  • Trauma
  • Vasoplegia

NCT number NCT05146336
Study type Observational [Patient Registry]
Source CytoSorbents, Inc
Contact Marie-Christin Pawlik, PhD
Phone +49 30 654 99 145
Email cosmos@cytosorbents.com
Status Recruiting
Phase
Start date June 22, 2022
Completion date September 2032

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